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The study on the effects of different acupoint combinations with percutaneous electrical stimulation on postoperative nausea and vomiting in patients undergoing gynecological laparoscopic surgery

The study on the effects of different acupoint combinations with percutaneous electrical stimulation on postoperative nausea and vomiting in patients undergoing gynecological laparoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000914
Enrollment
Unknown
Registered
2025-05-07
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative nausea and vomiting

Interventions

Control group 0:Electrodes are applied to the corresponding acupuncture points but no electrical stimulation is given
Experiment Group 1:Neiguan acupoint + Hegu acupoint + Zusanli acupoint transcutaneous acupoint electrical stimulation
Experiment Group 2:Gongsun acupoint + Hegu acupoint + Zusanli acupoint transcutaneous electrical stimulation

Sponsors

Departmenrt of Anesthesiology General Hospital of Xinjiang military region
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1)Voluntarily participate in this study and sign the informed consent form; (2)American Society of Anesthesiologists (ASA) classification: I-II; (3)BMI: 18-30kg/m2; (4)No abnormalities in the functions of major organs (heart lungs liver kidneys); (5)No history of motion sickness Meniere's syndrome or otolith disease;

Exclusion criteria

Exclusion criteria: (1) Pregnant or breastfeeding; (2) Severe organic heart disease wearing a cardiac pacemaker cardioversion device or defibrillator; (3) Severe digestive tract diseases; (4) Mental retardation mental illness or neurological disease combined with mental and psychological illness or epilepsy history; (5) Anti-vomiting drugs vomiting-inducing drugs opioids or glucocorticoids were used within 3 days before surgery and anti-vomiting drugs antacid drugs or nausea and vomiting occurred within 24 hours before surgery; (6) Known allergy to the drug class of Stilamin or Dexamethasone or to the material of the electrode patch and the selected acupoint skin area shows rashes or local infections; (7) Serious complications during or after the surgery which make the subject's medical condition unstable or complicate the condition; (8) Patients participating in this study also participated in other clinical studies during the same period; (9) Patients voluntarily give up participating in the trial lose follow-up or die.

Design outcomes

Primary

MeasureTime frame
The overall incidence and severity of nausea and vomiting within 24 hours after surgery;

Secondary

MeasureTime frame
The occurrence of other complications during the patient's awakening period;Postoperative antiemetic drug use in patients;Hemodynamic changes during induction and maintenance of general anesthesia;The time of the patient's first gas bowel movements eating and getting out of bed after surgery;The VAS score of the patients at 30 min 12 h and 24 h after surgery;

Countries

China

Contacts

Public ContactJiancheng Huang

Departmenrt of Anesthesiology General Hospital of Xinjiang military region

Zyymzkhjc@sina.com+86 133 1980 6825

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026